Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Dimethylamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Dimethylamine SCHEMBL4224813 | 0.96 | — | — | |
| Dimethylamine SCHEMBL11617039 | 0.92 | — | — | |
| Diethylamine SCHEMBL11281613 | 0.77 | TP53 (0.57) | — | |
| Butane SCHEMBL28158603 | 0.77 | — | — | |
| Methyl Alcohol SCHEMBL1993580 | 0.73 | — | — | |
| Propane SCHEMBL10466038 | 0.71 | — | — | |
| Butane SCHEMBL3052765 | 0.71 | — | — | |
| Propane SCHEMBL28102545 | 0.71 | KDM4E (0.40) | — | |
| Propane SCHEMBL28102546 | 0.71 | — | — | |
| Alcohol SCHEMBL1992680 | 0.70 | — | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 46 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20080119662-A1 | One Spot Synthesis of Citalopram from 5-Cyanophthalide | JUBILANT ORGANOSYS LIMTED (IN) | 2008-05-22 | — | — | US | claimed |
| EP-1723133-A1 | ONE POT SYNTHESIS OF CITALOPRAM FROM 5-CYANOPHTHALIDE | Jubilant Organosys Limited (IN) | 2006-11-22 | — | — | EP | claimed |
| WO-2005077927-A1 | ONE POT SYNTHESIS OF CITALOPRAM FROM 5-CYANOPHTHALIDE | JUBILANT ORGANOSYS LIMITED (IN) | 2005-08-25 | — | — | WO | claimed |
| WO-2004065375-A1 | PROCESSES FOR THE PREPARATION OF ESCITALOPRAM AND ITS PRECURSOR | NATCO PHARMA LIMITED (IN) | 2004-08-05 | — | — | WO | claimed |
| US-20160207942-A1 | METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF | UMICORE AG & CO. KG (DE) | 2016-07-21 | — | — | US | disclosed |
| US-8288569-B2 | Carbonyl asymmetric alkylation | SANDOZ AG (CH) | 2012-10-16 | — | — | US | disclosed |
| EP-1966127-B1 | CARBONYL ASYMMETRIC ALKYLATION | SANDOZ AG (CH) | 2011-04-06 | — | — | EP | disclosed |
| US-20110009648-A1 | Carbonyl Asymmetric Alkylation | SANDOZ AG (CH) | 2011-01-13 | — | — | US | disclosed |
| US-7767840-B2 | Organometallic compounds | ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) | 2010-08-03 | — | — | US | disclosed |
| US-20090156852-A1 | Organometallic compounds | ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) | 2009-06-18 | — | — | US | disclosed |
| EP-1682526-B1 | METHOD FOR THE PREPARATION OF CITALOPRAM | ADORKEM TECHNOLOGY SPA (IT) | 2009-01-14 | — | — | EP | disclosed |
| EP-1464724-B1 | Organometallic germanium compounds suitable for use in vapor deposition processes | ROHM & HAAS ELECT MAT (US) | 2008-12-10 | — | — | EP | disclosed |
| US-6579993-B2 | Halogenating 5-cyanophthalide to a cyanobenzeneacyl halide derivative reacted with organometallic 4-fluorophenyl halides and 4-fluorophenylboranes to a biphenyl ketone reacted with an organometallic 3-dimethylaminopropyl halide | ORION CORPORATION, FERMION (FI) | 2003-06-17 | — | — | US | disclosed |
| EP-1288211-A1 | Improved process for the manufacture of citalopram hydrobromide from 5-bromophthalide | Sekhsaria Chemicals Ltd. (IN) | 2003-03-05 | — | — | EP | disclosed |
| WO-2002066453-A1 | PROCESS FOR THE PREPARATION OF CITALOPRAM | NATCO PHARMA LIMITED (IN) | 2002-08-29 | — | — | WO | disclosed |
| US-20020115872-A1 | Process for the preparation of 1-(3-dimethylaminopropyl)-1-(4-Fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile | ORION CORPORATION FERMION (FI) | 2002-08-22 | — | — | US | disclosed |
| WO-2002060886-A1 | PROCESS FOR THE PREPARATION OF 1-(3-DIMETHYLAMINOPROPYL)-1-(4-FLUOROPHENYL)-1,3-DIHYDROISOBENZOFURAN-5-CARBONITRILE | ORION CORPORATION, FERMION (FI) | 2002-08-08 | — | — | WO | disclosed |
| US-4235820-A | Process for dibenzocycloheptene compounds | MERCK & CO., INC. (US) | 1980-11-25 | — | — | US | disclosed |
| US-4113726-A | HYPOTENSIVE AGENTS | E. R. SQUIBB & SONS, INC. (US) | 1978-09-12 | — | — | US | disclosed |
| US-3984419-A | HYPOTENSIVES | E. R. SQUIBB & SONS, INC. (US) | 1976-10-05 | — | — | US | disclosed |